Reaction Details |
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Target | Cannabinoid receptor 1 |
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Ligand | BDBM50415335 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_605642 (CHEMBL1070564) |
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EC50 | >31622.78±n/a nM |
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Citation | Gleave, RJ; Beswick, PJ; Brown, AJ; Giblin, GM; Goldsmith, P; Haslam, CP; Mitchell, WL; Nicholson, NH; Page, LW; Patel, S; Roomans, S; Slingsby, BP; Swarbrick, ME Synthesis and evaluation of 3-amino-6-aryl-pyridazines as selective CB(2) agonists for the treatment of inflammatory pain. Bioorg Med Chem Lett20:465-8 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cannabinoid receptor 1 |
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Name: | Cannabinoid receptor 1 |
Synonyms: | CANN6 | CANNABINOID CB1 | CB-R | CB1 | CNR | CNR1 | CNR1_HUMAN | Cannabinoid CB1 receptor | Cannabinoid receptor | Cannabinoid receptor 1 (CB1) | Cannabinoid receptor 1 (brain) |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 52868.96 |
Organism: | Homo sapiens (Human) |
Description: | P21554 |
Residue: | 472 |
Sequence: | MKSILDGLADTTFRTITTDLLYVGSNDIQYEDIKGDMASKLGYFPQKFPLTSFRGSPFQE
KMTAGDNPQLVPADQVNITEFYNKSLSSFKENEENIQCGENFMDIECFMVLNPSQQLAIA
VLSLTLGTFTVLENLLVLCVILHSRSLRCRPSYHFIGSLAVADLLGSVIFVYSFIDFHVF
HRKDSRNVFLFKLGGVTASFTASVGSLFLTAIDRYISIHRPLAYKRIVTRPKAVVAFCLM
WTIAIVIAVLPLLGWNCEKLQSVCSDIFPHIDETYLMFWIGVTSVLLLFIVYAYMYILWK
AHSHAVRMIQRGTQKSIIIHTSEDGKVQVTRPDQARMDIRLAKTLVLILVVLIICWGPLL
AIMVYDVFGKMNKLIKTVFAFCSMLCLLNSTVNPIIYALRSKDLRHAFRSMFPSCEGTAQ
PLDNSMGDSDCLHKHANNAASVHRAAESCIKSTVKIAKVTMSVSTDTSAEAL
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BDBM50415335 |
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n/a |
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Name | BDBM50415335 |
Synonyms: | CHEMBL596569 |
Type | Small organic molecule |
Emp. Form. | C14H13Cl2N3O |
Mol. Mass. | 310.179 |
SMILES | Clc1ccc(Cl)c(c1)-c1ccc(nn1)N1CCOCC1 |
Structure |
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